Publications for Jenny Welander
Co-author map based on ISI articles 2007-

Publications mentioned in social media 22 times*


yap1 tumors sporadic somatic sequencing pheochromocytomas pheochromocytoma pccs patients paraganglioma nf1 mutation marker lines genetics gene epas1 dna cetuximab cells

Journal Articles

Adam Stenman, Fredrika Svahn, Jenny Welander, Boel Gustavson, Peter Söderkvist, Oliver Gimm and C Christofer Juhlin
  Immunohistochemical NF1 Analysis Does not Predict NF1 Gene Mutation Status in Pheochromocytoma.
  Endocrine pathology, 2015, 26(1), 9-14.

C. Christofer Juhlin, Adam Stenman, Felix Haglund, Victoria E. Clark, Taylor C. Brown, Jacob Baranoski, Kaya Bilguvar, Gerald Goh, Jenny Welander, Fredrika Svahn, Jill C. Rubinstein, Stefano Caramuta, Katsuhito Yasuno, Murat Guenel, Martin Backdahl, Oliver Gimm, Peter Söderkvist, Manju L. Prasad, Reju Korah, Richard P. Lifton and Tobias Carling
  Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene
Altmetric usage: 3

  Genes, Chromosomes and Cancer, 2015, 54(9), 542-554.
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Fredrik Jerhammar, Ann-Charlotte Johansson, Rebecca Ceder, Jenny Welander, Agneta Jansson, Roland C. Grafstrom, Peter Söderkvist and Karin Roberg
  YAP1 is a potential biomarker for cetuximab resistance in head and neck cancer
  Oral Oncology, 2014, 50(9), 832-839.
 Web of Science® Times Cited: 5

Johan Kugelberg, Jenny Welander, Francesca Schiavi, Ambrogio Fassina, Martin Backdahl, Catharina Larsson, Giuseppe Opocher, Peter Söderkvist, Patricia L. Dahia, Hartmut P. H. Neumann and Oliver Gimm
  Role of SDHAF2 and SDHD in von Hippel-Lindau Associated Pheochromocytomas
Altmetric usage: 2

  World Journal of Surgery, 2014, 38(3), 724-732.
   Fulltext  PDF  
 Web of Science® Times Cited: 1

Ravi Kumar Dutta, Jenny Welander, Michael Brauckhoff, Martin Walz, Piero Alesina, Thomas Arnesen, Peter Söderkvist and Oliver Gimm
  Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas
  Endocrine-Related Cancer, 2014, 21(1), L1-L4.
   Fulltext  PDF  
 Web of Science® Times Cited: 1

Jenny Welander, Adam Andreasson, C. Christofer Juhlin, Roger W. Wiseman, Martin Backdahl, Anders Hoog, Catharina Larsson, Oliver Gimm and Peter Söderkvist
  Rare Germline Mutations Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma
Altmetric usage: 2

  Journal of Clinical Endocrinology and Metabolism, 2014, 99(7), E1352-E1360.
 Web of Science® Times Cited: 10

Jenny Welander, Adam Andreasson, Michael Brauckhoff, Martin Backdahl, Catharina Larsson, Oliver Gimm and Peter Söderkvist
  Frequent EPAS1/HIF2 alpha exons 9 and 12 mutations in non-familial pheochromocytoma
  Endocrine-Related Cancer, 2014, 21(3), 495-504.
 Web of Science® Times Cited: 3

Andreas O Tillmar, Barbara Dell'amico, Jenny Welander and Gunilla Holmlund
  A universal method for species identification of mammals utilizing next generation sequencing for the analysis of DNA mixtures
Altmetric usage: 14

  PLoS ONE, 2013, 8(12), e83761.
   Fulltext  PDF  
 Web of Science® Times Cited: 4

Jenny Welander, Peter Söderkvist and Oliver Gimm
  Editorial Material: The NF1 gene: a frequent mutational target in sporadic pheochromocytomas and beyond
  Endocrine-Related Cancer, 2013, 20(4), C13-C17.
 Web of Science® Times Cited: 3

Jenny Welander, Stina Garvin, Rickard Bohnmark, Lars Isaksson, Roger W. Wiseman, Peter Söderkvist and Oliver Gimm
  Editorial Material: Germline SDHA Mutation Detected by Next-Generation Sequencing in a Young Index Patient With Large Paraganglioma
  Journal of Clinical Endocrinology and Metabolism, 2013, 98(8), E1379-E1380.
 Web of Science® Times Cited: 7

Daniel Kling, Jenny Welander, Andreas Tillmar, Oivind Skare, Thore Egeland and Gunilla Holmlund
  DNA microarray as a tool in establishing genetic relatedness-Current status and future prospects
  Forensic Science International: Genetics, 2012, 6(3), 322-329.
 Web of Science® Times Cited: 4

Jenny Welander, Catharina Larsson, Martin Backdahl, Niyaz Niyaz, Tobias Sivlér, Michael Brauckhoff, Peter Söderkvist and Oliver Gimm
  Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas
Altmetric usage: 1

  Human Molecular Genetics, 2012, 21(26), 5406-5416.
 Web of Science® Times Cited: 27

Jenny Welander, Peter Söderkvist and Oliver Gimm
  Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas
  Endocrine-Related Cancer, 2011, 18(6), 253-276.
 Web of Science® Times Cited: 71

Conference Articles

Fredrik Jerhammar, Jenny Welander, A C Johansson, Peter Söderkvist and Karin Roberg
  Gene Copy Number as Predictive Marker for Cetuximab Resistance in Head and Neck Squamous Cell Carcinomas in EUROPEAN JOURNAL OF CANCER, vol 47, issue , pp S571-S571

Ph.D. Theses

Jenny Welander
  Genetic Alterations in Pheochromocytoma and Paraganglioma

  Fulltext PDF

* Social media data based on publications from 2011 to present and with a DOI; data delivered by